Stomach peristalsis device and method

ABSTRACT

The invention relates to an implantable stomach prosthesis for surgically replacing or augmenting all or part of the antrum and/or pylorus of a stomach. The prosthesis controls the passage of food from the stomach to the small intestine. The prosthesis may be configured to chum ingested material and release it from the stomach through a prosthetic pyloric valve. At least one expandable member is arranged to be expanded to control the passage of food and/or to mimic the churning action of a patient&#39;s stomach. The prosthesis includes an outer support structure, a flexible inner member forming a conduit for the movement of material, and at least one expandable member located between the outer support structure and inner member. An implantable pump system is provided for inflating and deflating the expandable member(s).

FIELD OF THE INVENTION

The invention relates to a stomach prosthesis for the mixing ofmaterials in the stomach and/or the transport of materials through thestomach. In particular, the invention relates to a prosthetic stomachfor replacing or augmenting a portion of the stomach, e.g., the pylorusand/or antrum.

BACKGROUND OF THE INVENTION

In general when food is ingested into the stomach, initially, theelastic upper portion or fundus accommodates the food and the fundusexpands. As food enters and the fundus expands there is a pressuregradient created in the stomach between the fundus and the antrum(fundus pylori). A number of things occur at this time. Fluids tend tobe pushed through the pylorus, which acts as a leaky valve. Peristalticcontractions move down the stomach from the fundus into the antrum tomix and break down food and propel small particles through the pylorusinto the duodenum. In healthy human stomachs, peristalsis is believed tobe controlled at least in part by a region of the stomach identifiednear the interface of the fundus and the corpus along the greatercurvature. In this region, there are cells believed to govern theorgans' periodic contractile behavior that generate and propagaterhythmic electrical signals that correspond to the contractile behaviorof the stomach. These characteristic contractions are believed tocreate, a pressure gradient between the fundus pylori (or antrum) andduodenum that relates to the rate of gastric emptying. When thecontractions begin, the pylorus is generally closed, although fluid andsmall particles leak through the valve. As contractions or electricalactivity corresponding to the contractions reach pylorus, the pylorusbegins to open or relax. Thus, as the stomach churns and breaks downfood in a healthy stomach, the pylorus opens. As this is occurring,there may be electrically activity in the duodenum as well. Retrogradeelectrical activity from the duodenum, i.e. contractions or electricalactivity in the direction of the pylorus tends to cause the pylorus toclose, thus preventing bile and pancreatic juices from backing up intothe stomach. Accordingly, the opening and closing of the pylorus isinfluenced by input from both of its ends.

In a number of disease states or conditions, the contractions of thestomach and/or the opening and closing of the pylorus is irregular.Gastroparesis may result in insufficient contractions to chum food, movefood through the pylorus, and/or open the pylorus, among other things,resulting in gastro retention of food. In another motility disorderknown as dumping syndrome, the stomach empties at an abnormally highrate into the small intestine causing various gastrointestinaldisorders. It is also believed that obesity may be treated by alteringgastric motility or by causing the stomach to retain food for a greaterduration to slow gastric emptying.

Accordingly, it would be desirable to provide a device and method fortreating motility disorders of the stomach and/or obesity.

In some disease states, portions of the stomach and/or pylorus do notfunction properly or may require resection. Accordingly, it would bedesirable to provide a prosthetic stomach for replacing or augmentingall or part of a stomach and/or pylorus.

SUMMARY OF THE INVENTION

The present invention provides a prosthesis device and method forreplacing or augmenting all or part of the pylorus or antrum of thestomach.

In one embodiment, the prosthesis is designed to facilitate or expeditemixing or breaking down of food matter or liquids in the stomach. Inanother embodiment, the prosthesis is designed to control, facilitate orexpedite movement of food matter or liquids through the pylorus and intothe small intestine. In another embodiment, the prosthesis is designedto delay passage of food from the stomach and into the small intestine.

One embodiment of the present invention provides an implantable stomachprosthesis for surgically replacing all or part of the antrum andpylorus of a stomach. The stomach prosthesis is configured to churningested material and release it from the stomach through a prostheticpyloric valve. In one embodiment a plurality of expandable members arearranged to be expanded in a sequence that mimics the churning action ofa patient's stomach. The stomach prosthesis includes an outer supportstructure to be sewn on one end to the upper portion of the stomach andan opposite end to the duodenum. The prosthesis further includes anexpandable member or members located within the outer support structure,and a flexible inner member forming a conduit for the movement ofmaterial. The flexible inner member is located within the outer memberand the expandable member or members are located between the innermember and the outer support structure. The expandable members areexpanded and contracted, or inflated and deflated to provide a pumpingaction that chums and breaks down the material and pumps it through theprosthetic pylorus. The expandable members are isolated from thematerial moving through the prosthesis by the inner member in which allthe material is contained. Thus, the material does not get caught in theinterstices around the expandable members. The prosthetic pylorus, atthe exit point of the stomach, is also isolated from the material by theinner member.

In one embodiment of the invention, the implantable prosthesis furthercomprises an implantable pump system that includes a pump and aprogrammable controller. According to this embodiment, the expandablemembers are balloons configured to receive an inflation medium to expandthe expandable members. The implantable pump system includes a reservoirof sterile inflation medium used to inflate the various expandablemembers. The reservoir may be implantable separate from the pump, e.g.in soft tissue. In general, the pump system is a closed system where theinflation medium is stored or transported as it is pumped from oneinflation member to another. The prosthesis may be divided along itslength into sections. A section may include a single expandable memberor a plurality of expandable members that may be separately inflated ormay share a conduit coupled to a single output port and valve on thepump. Preferably, each of the expandable members or sections ofexpandable members has an input port and valve coupled to the pump suchthat only one valve is opened at a time. However, the system mayalternatively have more than one valve open at a time.

The controller controls the inflation and deflation of the expandablemembers by controlling the opening and closing of the valves coupled toeach of the expandable members, and by controlling the pump directionand pressurization of the expandable members. In one embodiment, theinflatable members are inflated to a predetermined pressure. The pumpmay determine the inflation pressure by monitoring the pumping action orwork of its motor. The inflation pressure may also be sensed by sensorsthat sense the pressure of the system, e.g. in the fluid header of thepump system. According to one embodiment, in a first churning mode, afirst section of expandable members corresponding to a first section ofthe antrum is inflated, then a second adjacent section is inflated. Thesecond section is inflated before the first section is deflated so thatthe material in the prosthesis cannot move back in an orad directionwhen the second section is inflated a number of subsequent inflationmember sections may then be inflated and deflated in a manner thatmimics the stomach's mixing and churning of food material. In this mode,the prosthetic pyloric valve may be partially open to permit liquid andsmall particles to pass through the pylorus into the small intestine.

A second mode may be employed to empty the stomach. According to oneembodiment of this second mode, a first section of expandable memberscorresponding to a first section of the antrum is inflated, then asecond adjacent section is inflated. The second section is inflatedbefore the first section is deflated so that the material in theprosthesis cannot move back in an orad direction when the second sectionis inflated. The first section is then deflated. Then the third sectionis inflated, etc. until the section adjacent the pylorus is inflated.According to this mode the pylorus may be opened further to permitpassage of more food material. If the food has not been sufficientlybroken down to pass through the pylorus, the churning mode may berepeated.

In either of these modes sensors may be employed on each side of thepyloric valve to sense pressure or changes in pressure. The pyloricvalve may be relaxed or tightened depending on the sensed pressure. Forexample, if there is an increased pressure from the duodenum side of thepyloric valve, the pyloric valve is tightened to prevent back flow ofmaterial, e.g., bile, from the small intestine. If there is an increasedpressure from the stomach side of the pyloric valve, the valve may berelaxed to permit movement of material from the stomach into the smallintestine.

The controller may also control selection of a section of the stomachorgan for the churning or breaking down of material. The controller maycontrol selection of sections of the organ for peristaltic movement ormoving material through the stomach organ. Accordingly, sections may beselected according to a desired sequence of the section actuation. Thecontroller may be preprogrammed to control the peristalsis pattern ormay be reprogrammed externally or in response to sensed conditions atvarious locations in the prosthesis. For example the sensors may sensepresence or absence of material in the prosthesis and may direct apattern of peristaltic movement in the various sections accordingly.

In one embodiment, a single electromechanical device actuates theopening and closing of the valves according to the sequence. The valveactuator selectively actuates a particular valve at a given timeaccording to instructions from the controller.

The pump and the valve actuating mechanism may be powered through a coilinductively coupled transcutaneously to an external power source, or bya battery rechargeable through such coil and external power source.According to one embodiment, a user positions and actuates the externalpower source to actuate the prosthesis. The electronics unit may bepowered by a rechargeable or replaceable battery as the controllerconsumes relatively little power in its operation.

In another embodiment, the prosthesis is a prosthetic pyloric valve.According to this embodiment, a pyloric valve is replaced with aprosthesis comprising an outer member, an inner member and one or moresections of inflatable members between the outer and inner member. Theinflatable member sections are selectively inflated and deflated tocontrol the opening and closing of the pylorus. The prosthesis mayinclude pressure sensors on opposite ends of the valve. The pressuresensors sense pressure in the stomach and duodenum and the opening andclosing of the valve is adjusted accordingly. For example, a pressureincrease from the duodenum would trigger the closure of the valve toprevent backflow of material into the stomach. An increasing pressurefrom the stomach may trigger a relaxing of the valve to permit materialsto pass out of the stomach.

In another embodiment, the natural pyloric valve is augmented byimplanting a pyloric prosthesis in the duodenum adjacent the pyloricvalve. In this embodiment, the prosthesis may act to prevent materialfrom passing into the small intestine even when the natural pyloricvalve is open. Thus the augmented prosthetic pylorus may be used toretain food in the stomach for a greater length of time, e.g., toprevent gastric dumping or to treat obesity. According to thisembodiment, one or more inflatable members sections are provided betweenan inner member and an outer member. The outer member is sutured ontothe inside of the duodenum intestinal wall, just below the pylorus.Inflation conduits extend from the expandable member out of the outersupport member and intestine. The conduits are coupled to an implantedpump that inflates and deflates the inflation member sections as desiredto retain or pass food.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a side view of a prosthetic stomach device attached to astomach according to an embodiment of the invention.

FIGS. 1B and 1B-1 are schematic side views of the prosthesis of FIG. 1Ain a relaxed position, including a pump, valve actuating device andcontroller.

FIG. 1B-2 is an enlarged view of a portion of the prosthetic stomach ofFIG. 1B illustrating the wire sensors.

FIG. 1C is a cross-section of FIG. 1B along the lines 1C-1C.

FIG. 1D is a cross-section FIG. 1B along the lines 1D-1D.

FIG. 1E is a schematic side view of the prosthesis of FIG. 1A a firstactuated position.

FIG. 1F is a schematic side view of the prosthesis of FIG. 1A in anotheractuated position.

FIG. 1G is a schematic side view of the prosthesis of FIG. 1A in anotheractuated position.

FIG. 1H is a schematic side view of the prosthesis of FIG. 1A in anotheractuated position.

FIG. 1I is a schematic side view of the prosthesis of FIG. 1A in anotheractuated position.

FIG. 1J is a schematic side view of the prosthesis of FIG. 1A in anotheractuated position.

FIG. 2A is a side view of a prosthetic stomach device attached to astomach according to an embodiment of the invention.

FIG. 2B is a schematic side view of the prosthesis of FIG. 2A in arelaxed position.

FIG. 2C is a schematic side view of the prosthesis of FIG. 2A in aclosed position.

FIG. 3A is a schematic side view of a prosthetic stomach device attachedto a stomach according to another embodiment of the invention.

FIG. 3B is a schematic side view of the prosthesis of FIG. 3A in arelaxed position.

FIG. 3C is a schematic side view of the prosthesis of FIG. 3A in aclosed position.

FIG. 4 is a schematic of a miniature valve-actuating device forcontrolling the valves of the pump of an embodiment of the invention ina first position with a valve closed and a rotational position in whichnone of the openings of the device are aligned with a valve.

FIG. 4A is an end view of the device as illustrated in FIG. 4 in thefirst position.

FIG. 5 is a schematic of the valve-actuating device of FIG. 4 in asecond position.

FIG. 5A is an end view of the device illustrated in FIG. 5 with thevalve open and an inflation being inflated.

FIG. 6 is a schematic of the micro valve-actuating device in therotational position of FIG. 5 with the valve closed and the inflationmember in an inflated position.

FIG. 6A is an end view of the device illustrated in FIG. 6.

FIG. 6B is a schematic side cross-section of the cylinder and rod ofFIG. 6.

FIG. 6C is a cross section of FIG. 6B along the lines 6B-6B.

FIG. 6D is a cross section of FIG. 6B along the lines 6D-6D.

FIG. 6E is a top view of the cylinder of FIG. 6.

FIG. 6F is a cross section of a portion of the cylinder as illustrate inFIG. 6E along the lines 6F-6F.

DETAILED DESCRIPTION OF THE INVENTION

Referring to FIG. 1A, a prosthetic stomach 30 is illustrated attached tothe upper portion 201 of the stomach 200 at the orad end portion 33 ofthe prosthetic stomach 30 and to the duodenum 202 at the aborad endportion 34 of the prosthetic stomach 30. An implantable pump system 40(FIG. 1B-1) and electronics unit 50 (FIG. 1B-1) are contained in ahousing 80 coupled to the prosthetic stomach 30. The pump system 40 andelectronics unit control the inflation and deflation of inflatablemembers 36 a-g (FIG. 1B) that are inflated and deflated according to adesired protocol, to actuate the stomach prosthesis 30. A bladder 49 ofthe pump system 40 is located externally of the housing, within thepatient's soft tissue.

A schematic of the prosthesis of one embodiment is illustrated in FIGS.1A-1J. The prosthesis includes a prosthetic stomach 30, a hermeticallysealed pump system 40 and a hermetically sealed electronics unit 50including a controller 51 for controlling the pump system 40. The pumpsystem 40 and electronics unit 50 may be contained in the same housing80 illustrated in FIG. 1A or may alternatively be separate.

The prosthetic stomach 30 includes an outer support member 31, a seriesof inflatable member sections 36 a-g, and an inner member 32. Theinflatable member sections 36 a-g each comprise a plurality of opposinginflatable members that when inflated act to close together and squeezethe inner member 32. Each inflation member section 36 a-f corresponds toa particular section a-f of the prosthetic stomach 30. In thisparticular embodiment, inflatable member sections 36 a-d each comprisethree inflatable members where the prosthetic stomach 30 is larger (SeeFIG. 1C), and inflatable member sections 36 e-g each comprise twoinflatable members where the prosthetic stomach 30 is narrow (See FIG.1D).

The outer support member 31 comprises a flexible, relatively inelasticmaterial such as, for example, polyethylene or polyurethane, andprovides structural support for the prosthetic stomach 30 (alternativelyan elastic material may be used). The prosthesis sections a-f andinflatable member sections 36 a-f form an antrum portion 37 of thestomach. Section g and inflatable member section 36 g form a prostheticpyloric valve 38 at the aborad end portion 34 of the stomach prosthesis30. The inner member 32 comprises a thin-walled, non-elastic flexiblematerial such as polyethylene or polyurethane. The inside of the innermember 32 may be coated with an antibiotic surface, such as a silvercoating, to reduce bacterial growth. The inner member 32 is attached tothe outer support member 31 at the orad end portion 33 and the aboradend portion 34 of the prosthetic stomach 30 (for example, by welding) toprovide an isolated cavity where material is mixed, broken down andpassed through the pyloric valve 38. The orad end portion 33 of theouter support member 31 includes an extended portion for suturing theouter support member 31 to the upper portion of the stomach 201. Theinflatable member sections 36 a-g are located between the outer supportmember 31 and the inner member 32. The inner member 32 floats relativelyloosely within the outer support member 31 so as to permit movementincluding the inflation and deflation of the inflatable member sections36 a-g.

Although sections 36 a-g are illustrated, the number of inflation membersections depend on a selected prosthesis size, the size of the patientor the amount of the stomach to be replaced.

Each of the inflation members of a section converge together wheninflated, to churn or move material in the prosthetic stomach 30. Eachinflatable member section 36 a-g is coupled to and is in fluidcommunication with a corresponding one of conduits 39 a-g, respectively.Conduits 39 a-g are used to selectively deliver inflation medium to andfrom inflatable members 36 a-g by an implanted pump system 40.

As illustrated in FIG. 1B, a controller 51 of an electronics unit 50controls the implantable pump system 40 to selectively inflate anddeflate inflatable member sections 36 a-g. The pump system 40 includes abi-directional hydraulic pump 41 having an intake 47 coupled to a fluidreservoir 49 and an output 44 in fluid communication with a header 45having fluid ports 45 a-g. The bi-directional pump 41 may be configuredin a number of ways to provide pumping in two directions, for example,by controlling a series of valves that direct fluid into or out of thereservoir 49 or by providing a DC powered reversible pump. The fluidreservoir 49 contains a sterile, radiopaque inflation medium sufficientto inflate two sections of inflation members 36 a-g or a combinationthereof at a given time. The fluid reservoir 49 may be implanted at alocation adjacent to or away from the pump system 40 (e.g. in softtissue) or alternatively may be included with the pump system.

Each fluid port 45 a-g is coupled to a respective valve 46 a-g, which iscoupled to a respective conduit 39 a-g. Each conduit 39 a-g is coupledto a corresponding inflation member pair 36 a-g. The valves 46 a-g arecontrolled by a valve actuating device 300 which operation is controlledby the controller 51 of the electronics unit 50. The valves 46 a-g inthis particular embodiment are controlled by a electromechanical devicedescribed in more detail with reference to FIGS. 4-6F. Alternative valveactuating mechanisms are also contemplated, for example, individuallyoperated bistable solenoid valves may be used.

A pressure transducer 48 is located between the output 44 of the pump 41and the header 45. The pressure transducer 48 senses the pressure of thefluid of a particular section of inflation members when thecorresponding solenoid valve of the corresponding port is in an openposition. The pressure transducer 48 is coupled to the controller 51,which controls the pump 41 in response to a sensed pressure.

Sensors 53 and 54 are located on opposing ends of the inflation membersection 36 g (forming the pyloric valve 38) between the outer supportmember 31 and the inner member 32. Sensor 54 is located on the antrumside while sensor 54 is location on the duodenum side. The sensors 53,54 are coupled to the electronics unit 50 by leads. The sensors 53, 54are used to sense pressure on either side of the valve 38. When thepressure increases or reaches a threshold level on the stomach side ofthe valve 38, the pyloric valve is relaxed by partially deflating theinflation member section 36 g. When the pressure increases or reaches athreshold level on the duodenum side of the valve 38, the valve 38 istightened to prevent backflow into the stomach. The pressure sensors 53,54 are coupled to a controller which can compare the pressures sensed byeach of the sensors 53, 54 and provide a control signal that willcontrol the resulting desired inflation or deflation of the valve 38based on the sensed pressures or pressure differentials. The relativepressure on each side of the valve 38 as compared to the other side ofthe valve 38 may be used to control the valve 38 as well.

The electronics unit 50 includes a controller 51 and a battery 52powering the controller 51. The controller 51 is programmed to controlthe action of the various elements of the prosthesis and to respond tovarious sensed conditions. The controller 51 is coupled to the pumpsystem 40 and controls when and in which direction the pump 41 isactuated. The controller 51 is also coupled to a valve-actuating device300 that opens and closes the valves 46 a-g according to a programstored in the controller 51, thereby sequentially inflating anddeflating inflation member sections 36 a-g. According to one embodiment,only one valve is open at a time. The controller 51 also includes atelemetry coil 59 for communicating information to and receivinginformation from an external device. The external device may be used toprogram operation parameters into the controller 51. The external devicemay also receive signals from the controller 51 or electronics unit 50representative of various sensed conditions, e.g., pressure or systemleaks. The external device may program or reprogram the controller 51based on sensed parameters or other patient conditions. An externaldevice may also power the pump 41 and the valve-actuating device 300through an electronics unit 70 comprising an electromagnetic coil 71 forinductively receiving power from an external source. The electromagneticcoil 71 is coupled to the electronics unit 50, which includes a voltageregulating circuit. The electronics unit 50 and controller 51 controlthe pump 41 by powering the pump and controlling the valve actuatingdevice 300. The voltage regulating circuit of the electronics unit 50operates to convert a high frequency AC signal to a regulated voltagesignal that powers the pump 41 and valve actuating mechanism 300.Alternatively, coil 59 may be used for both powering the pump andelectronics unit 50 and for bi-directional telemetry communication.

The prosthetic stomach 30 also further includes wires 55 a-f (FIG. 1B-2)embedded in the prosthetic stomach 30 along its length and communicatingwith the electronic circuit 50. The wires 55 a and 55 d are located inthe outer tube 31 each between layers 31 i and 31 o and on opposingsides along the prosthetic stomach 30. Wires 55 b and 55 e are exposedbetween the inflation member pairs 36 a-e and the outer tube 31 onopposing sides along the prosthetic bowel 30. Wires 55 c and 55 f arelocated in the inner tube 32 along the stomach 30 between layer 32 i and32 o. Wire pairs 55 a and 55 d form an open circuit as do wire pairs 55b and 55 e, and wire pairs 55 c and 55 f. The electronic circuit 50 isconfigured to sense a large drop in impedance in one or more of thepairs wires 55 a-f, where a fluid closes the circuit of one or more ofthe wire pairs indicating potential leakage of fluid into, out of orwithin the stomach 30, e.g from material external the prosthetic stomach30, material within the inner member 32 of the stomach 30 or from aninflation member, or otherwise. In particular, a low impedance may bedetected by the controller 51, which is configured to sense impedancechanges in the wires 55 a-f. The impedance of the pairs of wires 55 a-fis periodically monitored by the controller 51. If a leak is detected apatient alarm may be triggered, e.g., by telemetrically delivering analarm signal from the electronics unit 50 to an external device.Furthermore, the location or cause of the leak may be determined bywhich wires 55 a-f have changed impedances. The wire pairs may be placedin different configurations within layers 31 i, 31 o, 32 i, 32 o orbetween the inner 32 and outer members 31, for example, they may be isparallel spiraled configurations to maximize the sensing of potentialleaks.

The prosthetic stomach 30 also includes a conduit 56 through theprosthetic bowel 30, into a port 57 inside the inner member 32 fordelivery a digestive enzyme, antibiotic material, or the like from areservoir 58. The reservoir 58 is coupled to the controller 51 and mayinclude a pump controlled by the controller 51 that provides a periodicor otherwise actuated (e.g. by a patient) injection of a material intothe inner member 32. The reservoir 58 may also be implanted in softtissue or may be included with the housing 180.

The prosthetic stomach 30 is illustrated in FIG. 1B in an inactiveposition in which a patient may ingest food and food may move from thefundus into the antrum portion 37 of the prosthetic stomach 30. In thisposition the pyloric valve 38 at the aborad end portion 34 is in aclosed position with inflation member section 36 g inflated. Theinflation member sections 36 a-f of the antrum portion 37 are relaxedand deflated.

FIGS. 1E-1J illustrate a sequence of mixing food and emptying theprosthetic stomach 30 of one embodiment of the invention. In FIG. 1E thevalve 46 a is opened and the pump 41 pumps inflation medium from thereservoir 49 into the inflation member section 36 a through the conduit39 a. The inflation member section 36 a is inflated to a predeterminedpressure as sensed by pressure transducer 48 or alternatively as sensedby the motor. Once the inflation member section 36 a is inflated, thevalve 46 a is closed by the valve actuating mechanism 60 (FIG. 1B).Inflation of the inflation member section 36 a closes the orad endportion 33 of the prosthetic stomach 30 from the upper portion of thestomach 201. Material within the prosthetic stomach 30 is thus containedin the antrum portion 37.

Next, as shown in FIG. 1F, inflation member section 36 b is inflated togrind material in the prosthetic stomach 30. The inflation membersection 36 b is inflated by opening the valve 46 b and inflating bypumping fluid from the reservoir 49 into inflation member section 36 bthrough conduit 39 b. Thus, the materials remain in the antrum portion37 without allowing them to move back in the direction of the inflationmember pair 36 a. The valve 46 b is then closed. The inflation membersection 36 b may then be deflated and other inflation member sections 36c-36 f may be inflated and deflated according to a predeterminedsequence to mix material in the antrum portion 37. As shown in FIGS. 1Eand 1F, the pyloric valve 38 is only slightly open, permitting fluids orsmall particles to pass through.

After some mixing has occurred, as illustrated in FIG. 1G, the pyloricvalve 38 may be further relaxed by partially deflating inflation membersection 36 g. Thus as inflation members are inflated in an aboraddirection, material that is sufficiently broken down may pass throughthe pyloric valve 38. In FIG. 1G, inflation member section 36 b isinflated. The inflation member 36 a has been deflated from a inflatedposition similar to that of FIG. 1F by selecting valve 46 a, reversingthe pump direction, pumping the inflation medium out of the inflationmember section 36 a back to the reservoir 49 and closing the valve 46 a.As shown in FIG. 1H, inflation member section 36 c is next inflated toadvance material further through the prosthetic stomach 30. Before theadjacent inflation member section 36 b is deflated, the inflation membersection 36 c is inflated by opening the valve 46 c and by pumping fluidfrom the reservoir 49 into inflation member section 36 c through conduit39 c. Thus, any materials are advanced further toward the pyloric valve38. The valve 46 c is then closed.

Referring to FIG. 1I, inflation member section 36 b has been deflated byselecting the valve 46 b, reversing the pump direction and pumping theinflation medium out of the inflation member pair 36 b and closing thevalve 46. The inflation member section 36 d is inflated by selecting thevalve 46 d and pumping inflation medium into the inflation membersection 36 d. A number of inflation member sections may be provided inthe prosthetic stomach 30 and the sequence of inflating and deflatingthe inflation members continues until the last inflation member sections36 e and 36 f are inflated as illustrated in FIG. 1J.

If the materials have not been sufficiently broken down to pass throughthe pyloric valve 38 the mixing cycle may be repeated until they aresufficiently broken down.

FIGS. 4-6F illustrate a valve-actuating device 300 according to anembodiment of the invention. The valve-actuating device 300 comprises acylinder 310 having a length Lc aligned parallel with the length Lh ofthe header 45 of the pump 41 and adjacent the valves 46 a-g. Thecylinder 310 includes a plurality of openings 320 a-g, spaced a defineddistance along the length Lc of the cylinder 310 with respect to theother openings so that each opening is aligned lengthwise with acorresponding one of the valves 46 a-g. Each opening 320 a-g is alsospaced a defined discrete distance circumferentially from the otheropenings. The cylinder 310 is coupled to a stepper motor 330 thatrotates the cylinder 310 according to instructions from the controller51 (FIG. 1A) into discrete circumferential positions to interfacinglyalign a selected opening with a corresponding selected valve. Thus, thecylinder 310 may be rotated to discrete positions wherein in eachposition one of the openings 320 a-g is interfacing a corresponding oneof the valves 46 a-g to be actuated.

A valve is actuated by a peg extending out of an interfacing opening inthe cylinder 310 to engage and move the valve into an open position.Each opening 320 a-g in the cylinder 310 includes concentricallymoveable peg 321 a-g respectively. Each of the pegs 321 a-g is capableof being partially advanced in a circumferential direction out of thecorresponding opening 320 a-g in the cylinder 310. When interfacing witha corresponding valve 46 a-g, a corresponding peg 321 a-g may beadvanced to engage and open the corresponding valve 46 a-g to open it.

Once a valve is selected and the controller 51 instructs the steppermotor 330 to rotatably position the cylinder 310 accordingly, anactuating rod 323 is advanced through the cylinder 310 to engage andadvance the corresponding aligned, interfacing peg out of the cylinder310 to open the corresponding valve.

The actuating rod 323 slidably extends axially through an axial opening313 in the cylinder 310. The rod 323 is coupled to a solenoid 328 thatmoves the rod 323 between two positions: a first resting position (FIG.4-4A, FIGS. 6-6F) and a second valve actuating position (FIG. 5-5A). Thesolenoid 328 advances and retracts the rod 323 to and from a valveactuating position. The actuating rod 323 moves in a direction generallyperpendicular to the circumferential sliding direction of the pegs 321a-g. The actuating rod 323 includes a central rod 324 and a plurality ofstaggered fins 325 a-g having cammed surfaces 326 a-g. In the firstposition, the fins 325 a-g are staggered in a lengthwise relationshipbetween the valves 46 a-g and a second position, the fins 325 a-g aregenerally aligned in a lengthwise relationship with the valves 46 a-g.The cammed surfaces 326 a-g are arranged so that when the rod 323 isadvanced to the second position, a corresponding one of the cammedsurfaces 326 a-g will engage a corresponding one of the pegs 321 a-g tomove the corresponding one of the pegs 321 a-g circumferentially out ofa corresponding one of the openings 320 a-g.

The axial opening 313 through the cylinder 310 includes a central rodportion 314 for receiving the rod 323 and a fin portion 315 forreceiving in the fins 325 a-g. The central rod portion 314 extendsaxially through the cylinder 310. The fin portion 315 of the axialopening 313 includes open portions 316 a-g staggered in a lengthwiserelationship between the valves 46 a-g. Each open portion 316 a-g isopen within the rod opening 313 about the circumference of the cylinder310 so that when the rod 323 is in the first position, the cylinder 310is free to rotate without interference of the fins 325 a-g. The finportion 315 also includes a plurality of slits 317 a-g circumferentiallyspaced from the other slits, wherein each slit extends longitudinallythrough the cylinder, between each of the open portions 316 a-g andperpendicularly through a corresponding one of the openings 320 a-g.

The fins 325 a-g are aligned in a position with the circumferentiallyextending top portions facing the header 45. The cylinder 310 may berotated when the rod 323 and fins 325 a-g are in the first position. Thecylinder when rotated to one of its discrete positions aligns acorresponding slit with the fins so that in the second position the finsadvance through that slit. When the fins 325 a-g are moved into thesecond position, the fins 325 a-g extend through the slit correspondingto the opening that is positioned in alignment with a correspondingvalve. In each discrete position the fins 325 a-g are aligned with aslit permitting the corresponding fin to slide into the opening andengage the pin moving the pin out of the opening engaging the correspondvalve with which it is aligned, thus actuating the corresponding valve.Each peg 321 a-g is biased by a corresponding spring (329 a only isshown) into a position circumferentially into the opening so that whenthe fins are retracted (e.g. FIG. 6), the pin moves back into theopening.

The controller 51 controls the timing and actuation of the cylinder 310rotation and the solenoid 328 positioning. Referring to FIG. 4, thecylinder 310 is rotated to a position in which none of the pegs arealigned with valve 36 a. The rod is in a first position in which thecylinder 310 may rotate freely. The cylinder 310 is then rotated asillustrated in FIG. 5 so that the opening 321 a is aligned with thevalve 46 a. The rod 323 is advanced so that the fins 325 a-g extendthrough the slit 317 a. Fin 325 a extends into the opening 320 a that isaligned with the slit 325 a and the cammed surface 326 a of the fin 325a engages the peg 321 a and advances it out of the opening 320 a toactuate valve 46 a. The valve 46 a is opened and the pump 41 pumps fluidfrom the reservoir 49 into the inflatable member pair 36 a. Asillustrated in FIG. 6, the rod 323 is then retracted releasing the peg321 a, which is biased by spring 329 a into the cylinder opening 320 a,and the valve 46 a is closed, leaving the inflation member pair 36 ainflated.

Referring to FIGS. 2A-2C another embodiment of the invention isillustrated. A prosthesis includes a prosthetic pylorus 130 and ahousing 180 containing a pump system similar to the pump system 40described above with reference to FIGS. 1A-1J. The prosthetic pylorus130 includes an outer support member 131, a series of inflatable membersections 136 a-b and an inner member 132. The outer support member 131comprises a flexible, relatively inelastic material such as, forexample, polyethylene or polyurethane, and provides structural supportfor the pylorus (elastic materials may be used as well.). The innermember 132 comprises a thin-walled, non-elastic flexible material suchas polyethylene or polyurethane. The inner member 132 may be coated withan antibiotic surface, such as a silver coating, to reduce bacterialgrowth. The inner member 132 is attached to the outer support member 131at the orad end portion 133 and the aborad end portion 134 of theprosthetic pylorus 130 (for example, by welding) to provide an isolatedconduit through which material may pass. The orad end portion 133 andaborad end portion 134 of the outer support member 131 includerelatively thicker portions for suturing the orad end portion 133 of theouter support member 131 to the stomach 100 and aborad end portion 134of the outer support member 131 to the small intestine 101 as shown inFIG. 2A. The inner member 132 defines a conduit through which materialpass from the stomach 100 into the small intestine 101. The inflatablemember sections 136 a-b are located between the outer support member 131and the inner member 132 with the inner member 132 floating relativelyloosely within the outer support member 131 so as to permit theinflatable member sections 136 a-b to expand and contract.

The prosthesis 130 is implanted to replace the pylorus of the stomach.The inflatable member sections 136 a-b and the inner member 132 form avalve 138. The inflatable members 136 a-b are attached to the inside ofthe outer support member 131 between the outer support member 131 andthe inner member 132 along the length of the prosthesis 130. Accordingto this embodiment, the inflatable member section 136 a forms an oradinflatable member pair and the inflatable member section 136 b forms anaborad inflatable member pair. Each section of inflatable membersconverges together when inflated, to close the valve 138. The valve 138is actuated by inflating sections 136 a-b, which causes the inner member132 to squeeze together to seal the conduit closed.

Each section 136 a-b is coupled to and is fluid communication with acorresponding respective one of conduits 139 a, 139 b. Conduits 139 a,139 b are used to selectively deliver inflation medium to and fromsections 136 a-b by an implanted pump system 140 (and valve actuator)and electronics unit 150 similar to the pump system 40 (and valveactuator 300) and electronics unit 50 described above with reference toFIGS. 1A-1J and FIGS. 4-6F.

Referring now to FIGS. 3A-3C, a supplemental pyloric valve 230 isillustrated implanted adjacent a pylorus 205 and in the duodenum 206.The supplemental pyloric valve 230 is coupled to an implanted housing280 including a hermetically sealed pump 241 and controller 251operating in a similar manner as pump system 40 (and valve actuator 300)and electronics unit 50 described above with reference to FIGS. 1A-J andFIGS. 4-6F

The supplemental pylorus 230 includes an outer support member 231, aseries of inflatable members sections 236 a-b and an inner member 232.The outer support member 231 comprises a flexible, relatively inelasticmaterial such as, for example, polyethylene or polyurethane, andprovides structural support for the pylorus (elastic materials may beused as well). The inner member 232 comprises a thin-walled, non-elasticflexible material such as polyethylene or polyurethane. The inner member232 may be coated with an antibiotic surface, such as a silver coating,to reduce bacterial growth. The inner member 232 is attached to theouter support member 231 at the orad end portion 233 and the aborad endportion 234 of the supplemental pyloric valve 230 (for example, bywelding) to provide an isolated conduit through which material may pass.The orad end portion 233 of the support member 231 is sutured on to theinner wall 207 of the duodenum adjacent the pylorus 205. The aborad endportion 234 of the outer support member 231 is sutured to duodenum 206downstream of the orad end portion as shown in FIG. 3A. The inner member232 defines a conduit through which material pass from the pylorus 205into the small intestine 206. The inflatable member sections 236 a-b arelocated between the outer support member 231 and the inner member 232with the inner member 232 floating relatively loosely within the outersupport member 231 so as to permit the inflatable member sections 236a-b to expand and contract.

The supplemental pyloric valve 230 is implanted to supplement thepylorus of the stomach by further controlling the exit of material fromthe stomach through the pylorus and into the duodenum. In one embodimentthis is done to retain food in the stomach for a greater duration totreat obesity and/or dumping syndrome. The inflatable member sections236 a-b and the inner member 232 form a valve 238. The inflatablemembers 236 a-b are attached to the inside of the outer support member231 between the outer support member 231 and the inner member 232 alongthe length of the prosthesis 230. According to this embodiment, theinflatable member section 236 a forms an orad inflatable member pair andthe inflatable member section 236 b forms an aborad inflatable memberpair. Each pair of inflatable members converges together when inflated,to close the valve 238. The valve 238 is actuated by inflating sections236 a-b, which causes the inner member 232 to squeeze together to sealthe conduit closed.

Each section 236 a-b is coupled to and is fluid communication with acorresponding respective one of conduits 239 a, 239 b. Conduits 239 a,239 b extend out of the duodenum and are coupled to the pump 241.Conduits 239 a, 239 b are used to selectively deliver inflation mediumto and from sections 236 a-b by an implanted pump and control controllersimilar to the pump system 40 and electronics unit 50 described abovewith reference to FIGS. 1A-1J and FIGS. 4-6F.

While the invention has been described with reference to particularembodiments, it will be understood to one skilled in the art thatvariations and modifications may be made in form and detail withoutdeparting from the spirit and scope of the invention.

For example, the invention may be practiced replacing or augmenting allor part of a portion of the digestive tract such as the bowel or smallintestine as described, for example in U.S. application entitled“IMPLANTABLE DIGESTIVE TRACT ORGAN” filed on even date herewith,incorporated herein by reference.

1-34. (canceled)
 35. An implantable digestive organ for moving materialsthrough a portion of the digestive tract comprising: a flexible innermember forming a conduit for the movement of material therethrough; anda peristalsis element operatively coupled to the inner member to cause aperistaltic action of the inner member to materials located within theinner member.